# Effect of curcumin and Garcinia kola on the cerebellum of the transected sciatic nerve of the diabetic rats: glial and neuronal evidence

**Authors:** Abdullah Hilmi Marangoz, Hala Mahgoub Hamour, Arife Ahsen Kaplan, Işınsu Alkan, Gamze Altun, Süleyman Kaplan

PMC · DOI: 10.3389/fnins.2026.1758544 · Frontiers in Neuroscience · 2026-02-16

## TL;DR

This study examines how curcumin and Garcinia kola affect the cerebellum in diabetic rats with sciatic nerve injury, focusing on glial and neuronal changes.

## Contribution

The study provides new insights into the neuroprotective effects of curcumin and Garcinia kola in a diabetic rat model with peripheral nerve injury.

## Key findings

- Curcumin reduced the volume fraction of the molecular layer compared to Garcinia kola and diabetic groups.
- Diabetes inhibited caspase-3 activity but also showed intense activation in control and curcumin-treated groups.
- Sciatic nerve injury combined with diabetes caused significant structural changes in the cerebellar cortex.

## Abstract

Peripheral nerve injury and diabetes can lead to some serious neurodegenerative changes in central nervous system structures. Curcumin and Garcinia kola are considered natural compounds with known antioxidant and neuroprotective properties. The current study aims to investigate the effects of curcumin and Garcinia kola on granular cells, glial cells, and Purkinje cells in a diabetic rat model induced by sciatic nerve transection, using stereological and immunohistochemical approaches.

Thirty-five male adult rats were divided into five groups: Control, Sham (Transected Sciatic Nerve), Transected Sciatic Nerve + Diabetes (T + DM), T + DM + Curcumin (T + DM + Cur), and T + DM + Garcinia kola (T + DM + GK). Ninety days after the sciatic nerve injury, the rats' cerebellar tissues were dissected and processed into paraffin and resin blocks. Volumetric fractions of cortical layers and white matter were estimated using the Cavalieri principle. Apoptosis and glial activation were assessed by immunohistochemical analysis.

Stereological analyses revealed that the volume fraction of the molecular layer was significantly lower in the T + DM + Cur group compared to the T + DM + GK and T + DM groups. A significant decrease in the volume fraction of the Purkinje cell layers was observed in the T + DM + Cur group compared to the Sham group. No significant differences were found between the groups in the granular layer and white matter volume fractions. Immunohistochemical analysis revealed inhibition of caspase-3 activity in the T + DM group. However, intense caspase-3 activation was also observed in the Control and T + DM + Cur groups.

Sciatic nerve transection, combined with diabetes, leads to significant structural and cellular changes in the cerebellar cortex. The mechanisms underlying the anti-apoptotic effects of diabetes on granular cells and other cerebellar components should be investigated in detail.

## Linked entities

- **Proteins:** Casp3 (caspase 3)
- **Chemicals:** curcumin (PubChem CID 969516)
- **Diseases:** diabetes (MONDO:0005015)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Bdnf (brain-derived neurotrophic factor) [NCBI Gene 24225], Pik3cb (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta) [NCBI Gene 85243], Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, Gfap (glial fibrillary acidic protein) [NCBI Gene 24387], Igf1 (insulin-like growth factor 1) [NCBI Gene 24482] {aka IGF}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], GK (glycerol kinase) [NCBI Gene 2710] {aka GK1, GKD}, Akt1 (AKT serine/threonine kinase 1) [NCBI Gene 24185] {aka Akt}
- **Diseases:** cerebellar degeneration (MESH:D013132), hypoxia (MESH:D000860), gestational diabetes (MESH:D016640), DM (MESH:D009223), Edema (MESH:D004487), central nervous system disorders (MESH:D002493), neuroinflammation (MESH:D000090862), Diabetes (MESH:D003920), cancer (MESH:D009369), Peripheral nerve injury (MESH:D059348), neurodegeneration (MESH:D019636), inflammation (MESH:D007249), Hyperglycemia (MESH:D006943), Cognitive problems (MESH:D003072), metabolic and chronic disease (MESH:D002908), peripheral nerve damage (MESH:D010523), Type 1 (MESH:D003922), neuronal damage (MESH:D009410), sciatic nerve (MESH:D020426), insulin resistance (MESH:D007333), infection (MESH:D007239), hypoglycemia (MESH:D007003), nerve injury (MESH:D000080902)
- **Chemicals:** toluidine blue (MESH:D014048), Cresyl violet (MESH:C028911), chlorhexidine (MESH:D002710), STZ (MESH:D013311), xylene (MESH:D014992), xylazine (MESH:D014991), garcinol (MESH:C054597), Paraffin (MESH:D010232), T (MESH:D014316), sodium chloride (MESH:D012965), glucose (MESH:D005947), ROS (MESH:D017382), eosin (MESH:D004801), glutaraldehyde (MESH:D005976), alcohol (MESH:D000438), paraformaldehyde (MESH:C003043), cefazolin sodium (MESH:D002437), resin (MESH:D012116), citrate (MESH:D019343), Ketalar (MESH:D007649), Hematoxylin (MESH:D006416), hydrogen peroxide (MESH:D006861), CUR (-), Curcumin (MESH:D003474)
- **Species:** Garcinia kola (species) [taxon 469930], Mus musculus (house mouse, species) [taxon 10090], Curcuma longa (turmeric, species) [taxon 136217], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950735/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950735/full.md

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Source: https://tomesphere.com/paper/PMC12950735